The 1-(13) C galactose breath test in GALT deficient patients distinguishes NBS detected variant patients but does not predict outcome in classical phenotypes
SourceJournal of Inherited Metabolic Disease, 43, 3, (2020), pp. 507-517
Article / Letter to editor
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Journal of Inherited Metabolic Disease
SubjectAll institutes and research themes of the Radboud University Medical Center; Radboudumc 6: Metabolic Disorders RIMLS: Radboud Institute for Molecular Life Sciences
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